Molina Ezequiel J, Ahmed Mustafa M, Sheikh Farooq H, Cleveland Joseph C, Goldstein Daniel J, Uriel Nir Y, Wang AiJia, Revis Jordan J, Mehra Mandeep R
Piedmont Heart Institute, Atlanta, Georgia, USA.
University of Florida, Gainesville, Florida, USA.
JACC Heart Fail. 2025 May;13(5):798-811. doi: 10.1016/j.jchf.2024.09.019. Epub 2024 Dec 18.
Prior analyses have suggested that a smaller left ventricular end-diastolic diameter (LVEDD) is associated with reduced survival following HeartMate 3 left ventricular assist device implantation.
In this trial-based comprehensive analysis, the authors sought to examine clinical characteristics and association with the outcome of this specific relationship.
The authors analyzed the presence of LVEDD <55 mm among 1,921 analyzable HeartMate 3 patients within the MOMENTUM 3 (Multicenter Study of MagLev Technology in Patients Undergoing Mechanical Circulatory Support Therapy With HeartMate 3) trial portfolio, on endpoints of overall survival and adverse events at 2 years. Adverse events included hemocompatibility-related (stroke, bleeding, and pump thrombosis) and non-hemocompatibility-related (right heart failure, infection) outcomes.
Those with a smaller LVEDD (<55 mm) (n = 108) were older (age 63 ± 11 years vs 60 ± 12 years; P = 0.005), were more often female (31% vs 20%; P = 0.096), and had more ischemic cardiomyopathy (60.2% vs 42.6%; P = 0.0004) compared with the LVEDD ≥55 mm group (n = 1,813). Death during implant hospitalization was higher (14.8 vs 5.7%; P = 0.0007) and survival at 2 years was lower (63.3% vs 81.8%; HR: 1.97 [95% CI: 1.39-2.79]; P = 0.0002) in the LVEDD <55 mm group. The LVEDD <55 mm group experienced more deaths due to hemocompatibility-related adverse events (2.8% vs 0.6%; HR: 4.61 [95% CI: 1.29-16.45]; P = 0.018) and right heart failure, both early (0-30 days; 7.4% vs 2.0%; HR: 3.70 [95% CI: 1.73-7.91]; P = 0.001) and late (>30 days; 12.0 vs 4.8%; HR: 2.58 [95% CI: 1.37-4.84]; P = 0.003). Low-flow alarms rehospitalizations were higher in the LVEDD <55 mm cohort (17.4 vs 8.3%; HR: 2.39 [95% CI: 1.59-3.59]; P < 0.001).
Although infrequent in occurrence, smaller LVEDD (<55 mm) is associated with increased risk for early and late mortality, a consequence of hemocompatibility-related and right heart failure-related deaths. Rehospitalizations due to low-flow alarms are also more frequent. (MOMENTUM 3 IDE Clinical Study Protocol [HM3™]; NCT02224755; MOMENTUM 3 Continued Access Protocol [MOMENTUM 3 CAP]; NCT02892955).
先前的分析表明,较小的左心室舒张末期内径(LVEDD)与植入HeartMate 3左心室辅助装置后的生存率降低有关。
在这项基于试验的综合分析中,作者试图研究这一特定关系的临床特征及其与结局的关联。
作者在MOMENTUM 3(使用HeartMate 3进行机械循环支持治疗的患者中磁悬浮技术的多中心研究)试验组合中的1921例可分析的HeartMate 3患者中分析LVEDD<55 mm的情况,以2年时的总生存率和不良事件为终点。不良事件包括血液相容性相关(中风、出血和泵血栓形成)和非血液相容性相关(右心衰竭、感染)结局。
与LVEDD≥55 mm组(n = 1813)相比,LVEDD较小(<55 mm)的患者(n = 108)年龄更大(63±11岁对60±12岁;P = 0.005),女性比例更高(31%对20%;P = 0.096),缺血性心肌病更多(60.2%对42.6%;P = 0.0004)。LVEDD<55 mm组植入住院期间的死亡率更高(14.8%对5.7%;P = 0.0007),2年生存率更低(63.3%对81.8%;HR:1.97 [95%CI:1.39 - 2.79];P = 0.0002)。LVEDD<55 mm组因血液相容性相关不良事件导致的死亡更多(2.8%对0.6%;HR:4.61 [95%CI:1.29 - 16.45];P = 0.018),以及右心衰竭,包括早期(0 - 30天;7.4%对2.0%;HR:3.70 [95%CI:1.73 - 7.91];P = 0.001)和晚期(>30天;12.0%对4.8%;HR:2.58 [95%CI:1.37 - 4.84];P = 0.003)。LVEDD<55 mm队列中因低流量警报再次住院的比例更高(17.4%对8.3%;HR:2.39 [95%CI:1.59 - 3.59];P < 0.001)。
尽管发生率较低,但较小的LVEDD(<55 mm)与早期和晚期死亡风险增加有关,这是血液相容性相关和右心衰竭相关死亡的结果。因低流量警报导致的再次住院也更频繁。(MOMENTUM 3 IDE临床研究方案[HM3™];NCT02224755;MOMENTUM 3持续接入方案[MOMENTUM 3 CAP];NCT02892955)